• 제목/요약/키워드: Stripping Voltammetry

검색결과 129건 처리시간 0.027초

폴리톨루이딘 합성 및 전기화학적 특성분석

  • 박수범;이성주;김은옥
    • 대한화학회지
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    • 제46권3호
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    • pp.225-228
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    • 2002
  • 폴리아닐린에 전자주게기(-CH3)를 치환하여 전자효과(electronic effect) 와 입체장애효과(steric effect)를 확인하기 위하여 폴리아닐린 유도체인 폴리톨루이딘(POT)1을 화학적 및 전기화학적으로 합성한 결과 입체장애효과가 더 우세하였다. 순환전압 전류법(Cyclic Voltammetry)과 전위차벗김 분석법(Constant Current Potentiometric Stripping Analysis)을 사용한 결과 POT의 IP는 4.95eV, EA는 3,24eV, Eg는 1.71eV임을 확인하였다.

Voltammetric Assay of Antibiotics for Modified Carbon Nanotube Sensor

  • Ly, Suw-Young;Yoo, Hai-Soo;Lee, Chang-Hyun
    • 한국응용과학기술학회지
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    • 제29권3호
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    • pp.443-449
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    • 2012
  • A investigation of electrochemical analysis of antibiotics Neomycin ($C_{23}H_{46}N_6O_{13}$) was searched using electrochemical square wave (SW) stripping and cyclic voltammetry (CV) using working sensor of the modified carbon nanotube combination electrodes, optimum diagnostic parameters were searched by anodic stripping, final conditions were attained to working range of 1.0-14.0 ng/L, detection limit (S/N) was found to be 0.6 ng/L. The developed method was discovered to be fitting in quality control in the food, pharmaceutical and other manufacturing sectors.

Geochemical speciation of dissolved heavy metals in acid mine drainage: effects of pH and total concentration

  • Jung, Hun-Bok;Yun, Seong-Taek;Kwon, Jang-Soon;So, Chil-Sup;Lee, Pyeong-Koo
    • 한국지하수토양환경학회:학술대회논문집
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    • 한국지하수토양환경학회 2003년도 추계학술발표회
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    • pp.404-408
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    • 2003
  • In this study, we examined the influences of pH and total concentration on the speciation of heavy metals (Cd, Cu, Zn) in acid mine drainage. Their labile concentrations were analyzed by Anodic Stripping Voltammetry (ASV) at both natural pH and adjusted pHs (from 2 to 8). We obtained regression equations for predicting labile concentrations as a function of the water pH and contamination level (total dissolved metal concentration). Our data show that labile Cu depends on both the total concentration and pH, while labile Cd and Zn concentrations are controlled mainly by their total concentration rather than pH. Therefore, the pH variation of AMD may significantly change the toxicity and bioavailability especially of Cu, owing to its speciation change.

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Electrochemical Determination of As(III) at Nanoporous Gold Electrodes with Controlled Surface Area

  • Seo, Min Ji;Kastro, Kanido Camerun;Kim, Jongwon
    • 대한화학회지
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    • 제63권1호
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    • pp.45-50
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    • 2019
  • Because arsenic (As) is a chemical substance toxic to humans, there have been extensive investigations on the development of As detection methods. In this study, the electrochemical determination of As on nanoporous gold (NPG) electrodes was investigated using anodic stripping voltammetry. The electrochemical surface area of the NPG electrodes was controlled by changing the reaction times during the anodization of Au for NPG preparation, and its effect on the electrochemical behavior during As detection was examined. The detection efficiency of the NPG electrodes improved as the roughness factor of the NPG electrodes increased up to around 100. A further increase in the surface area of the NPG electrodes resulted in a decrease of the detection efficiency due to high background current levels. The most efficient As detection efficiency was obtained on the NPG electrodes prepared with an anodization time of 50 s. The effects of the detection parameters and of the Cu interference in As detection were investigated and the NPG electrode was compared to flat Au electrodes.

희석 적정-순환전류전압법을 이용한 와트욕 내부 광택제 농도 모니터링 (Determination of brightener concentrations in Watt-type Ni Electroplating bath using dilution titration-cyclic voltammetry stripping (DT-CVS))

  • 최승회;권영환;이주열;김만;박영배;이규환
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2018년도 춘계학술대회 논문집
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    • pp.30-30
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    • 2018
  • 스마트 도금공장을 구축하기 위해서는 도금액 내부의 화학 물질 농도 변화를 측정할 수 있는 화학 센서 기술이 필수적으로 요구된다. 와트욕은 대표적인 고속 니켈 도금액 중 하나로 기본적으로 황산니켈, 염화니켈, 보릭산의 염과 함께 케리어(type-1 광택제), 광택제(type 2-광택제), 응력 제어제 등의 유기 첨가제로 구성되어 있다. 이러한 유기 첨가제는 전차된 니켈층의 두께 균일도, 조도, 미세 구조, 내부 응력 등 다양한 특성을 제어하며, 정밀한 농도 관리가 필수적으로 요구되나, 분석 기술의 부재로 인하여 지금까지도 대부분의 액관리는 할셀법이나 작업자의 경험에 의존하고 있다. Cyclic voltammetry stripping(CVS) 방법은 전기화학 분석 과정에서 나타나는 첨가제의 가속, 감속 특성 등과 여기에 수반되는 stripping peak의 변화를 이용하여 개별 첨가제의 농도를 측정하는 방법이며, 지금까지 인쇄회로기판의 비아필 공정, 전해 동박 제조, 반도체 배선 등 구리도금 산업 전반에 걸쳐 첨가제 관리에 효과적으로 적용되고 있다. 그러나 수소 발생으로 인한 stripping 효율 문제로 인하여 니켈, 주석, 아연 등 표준 환원 전위가 높은 금속 도금액 내부 첨가제 농도 측정은 아직 어려운 상황이다. 본 연구에서는 이 문제를 극복하기 위해 염소를 과량 첨가한 구리 도금액을 CVS 분석의 base 용액으로 이용하여 니켈 도금액 내부 여러 광택제 (polyetylene glycol(PEG) 계열, thiourea 계열, 2-butyne-1,4-diol 등) 농도를 측정하는 법을 제시하였다. 제시된 방법은 CVS 분석 과정에서 구리-염소 사이의 상호 작용으로 인해 생성되는 3가지 stripping peak의 상대적인 크기 변화가 첨가제 농도에 따라 영향을 받는다는 사실에 기반하였다. 본 연구에서는 여기에 관한 원인에 대해 고찰하였으며, 제시된 방법을 통해 광택제 계열 첨가제 농도 측정을 선택적으로 할 수 있다는 것을 증명하였다.

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DNA 고정 탄소나노튜브 페이스트전극의 물고기 세포속 테트라싸이클린에 정량 (Measuring Oxytetracycline Using a Simple Prepared DNA Immobilized on a Carbon Nanotube Paste Electrode in Fish Tissue)

  • 이수영;이장현;정영삼
    • 대한화학회지
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    • 제51권5호
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    • pp.412-417
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    • 2007
  • DNA를 고정한 탄소나노튜브 페이스트 전극으로 옥시테트라싸이클린 항생제의 분석조건을 연구하였다. 사각 파형 벗김 전압전류법과 순환 전압 전류법을 사용하여 최적조건에서 1-10 ngL?1의 정량 가능 범위에 도달하였다. 벗김법 0.1 mgL?1 농도에서 15번 반복 측정하여 0.068%의 상대표준편차였으며, 벗김법 최적 분석 조건에서 0.4 ngL?1의 검출 한계를 얻었다. 개발된 결과를 양식어류의 세포에서 응용하였다.

시차펄스 음극벗김 전압전류법에 의한 시안이온 측정의 감도향상 (Increased Sensitivity in Cyanide Measurement by Differential-Pulse Cathodic Stripping Voltammetry)

  • 나문선;권영순;채명준
    • 대한화학회지
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    • 제32권2호
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    • pp.130-134
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    • 1988
  • 수은방울전극에서 바로 시안이온을 시차펄스음극벗김 전압전류 법으로 측정한 결과 검출한계를 낮출수가 있었다. 가장 알맞는 실험조건은 다음과 같다. : 0.1M KCl-0.01M 인산염 지지전해질, pH 7, 석출전위 0.00V, 그리고 석출시간 3분이었다. 이 조건에서 검출한계는 $3{\times}10^{-7}M$ (8ppb) $CN^-$이다.

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비스무스코팅 탄소섬유전극과 갤릭산 착물을 사용한 구리 이온의 흔적량 분석 (Bismuth Coated Carbon Fiber Microelectrode with Gallic Acid n-Propyl Ester for Trace Copper Analysis)

  • 이수영;이장현;정영삼
    • 한국환경과학회지
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    • 제16권10호
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    • pp.1111-1118
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    • 2007
  • A bismuth-coated carbon fiber microelectrode was prepared using cyclic voltammetry (CV). An analytical application was performed for the copper analysis with Square Wave Stripping Voltammetry (SWSV). Gallic acid n-propyl ester (PG) was used for the complex formation with a copper ion, and electrochemical measurements were performed with a pre-amplifier of a low-current module for nano am per detection. The effects of various parameters on the response were optimized. Analytical working ranges of $0.03-25.9\;{\mu}gl^{-1}$ and $0-25\'mgl^{-1}$ Cu(II) were obtained. The relative standard deviation at $13\;mgl^{-1}$ Cu was 0.9% (n = 12) in optimum conditions. The detection limit was found to have been $0.019\;{\mu}gl^{-1}$, with a 30-sec accumulation time. The developed methods were applied to a copper assay in water samples.

Adsorptive Behavior of Catechol Violet and Its Thorium Complex on Mercury Electrode in Aqueous Media

  • Rabia Mostafa K. M.
    • 전기화학회지
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    • 제7권1호
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    • pp.9-15
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    • 2004
  • Cyclic voltammetry and chronocoulometry have been used for characterization of catechol violet (CV) at the hanging mercury drop electrode in acetic acid-sodium acetate buffer solution. At pH 2.94 a nearly symmetric cyclic voltammetric wave due to an irreversible weak adsorption of CV on mercury was obtained at concentration of $0.53{\mu}mol\;dm ^{-3}$. Under these conditions, CV adsorbes in a monolayer. Upon increasing the concentration, the symmetry of the wave decreases; it can be attributed to a mixed diffusion adsorption process. The amount of the adsorbed catechol violet on the HMDE expressed as surface concentration as well as the surface areaf occupied by one molecule$(\sigma)$ were calculated. It was found that the values obtained for f and o utilizing cyclic voltammetric and chrono-coulometry are almost identical. A 1:1 and 1:2 Th (IV)-CV complexes are formed on addition of thorium (IV) to catechol violet. These complexes are adsorbed and reduced on the HMDE at more negative potentials than the peak potential of free CV, Using the square-wave (SW) technique, the adsorptive cathodic stripping voltammetry, ACSV, of these complexes was studied. It was found that the SW-ACSV of Th(IV)-CV can be applied to the determination of thorium at the nanomole level. Optimum conditions and the analytical method of determination were presented and discussed.

Analysis of Cu in Mezcal Commercial Samples using Square Wave Anodic Stripping Voltammetry

  • Salinas, Gerardo;Ibanez, Jorge G.;Vasquez-Medrano, Ruben;Frontana-Uribe, Bernardo A.
    • Journal of Electrochemical Science and Technology
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    • 제9권4호
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    • pp.276-281
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    • 2018
  • High concentration of copper in mezcal, a representative Mexican spirituous alcoholic beverage, is a serious problem due to the damage that it may cause to human health. A cyclic voltammetry and square wave anodic stripping voltammetry study of copper (II) in three commercial mezcal samples based on glassy carbon electrode response was undertaken. The analysis was developed using a simulated matrix solution ($EtOH/H_2O$ (1:1), 0.1 M $LiClO_4$ and AcOH/AcONa 0.05 M/0.008 M), with Cu (II) concentrations in the range 0 - 1 ppm. Direct electrochemical analysis of mezcal samples was complicated by the presence of different organic compounds in the matrix. The analytical signal of Cu (II) in the spirituous was notably improved and the interferences caused by organic compounds were minimized, by diluting the mezcal samples 10% with $EtOH/H_2O$ (1:1) solution. An efficient quantification of Cu (II) was obtained from the calibration curve by the SWASV and using the internal standard method (Cd (II)) in commercial samples (1.2-6.7 ppm); the results were correlated satisfactorily with the values obtained by AAS.